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A case of retinocytoma Masamitsu Takeuchi 1 , Kanji Takahashi 1 , Masanobu Uyama 1 , Kiyoshi Yamamoto 2 , Hisashi Kusube 1Dept. of Ophthalmol, Kansai Med Univ 2Dept of Ophthalmol, Kishiwada City Hosp pp.685-688
Published Date 1987/6/15
DOI https://doi.org/10.11477/mf.1410210077
  • Abstract
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A solitary, non-symptomatic retinal tumor was detected in the left eye of a 18-year-old male. The tumor resembled retinoblastoma in its regressed state following irradiation. The tumor was located superior to the optic disc, was sharply demarcated, and was prominently elvated into the vitreous. It was grayish-white and showed a soft surface struc-ture without calcification. The tumor was surround-ed by atrophy and clumping of retinal pigment epithelium. Fluorescein angiography showed hypo-fluorescence in the early stage and dye staining of the tumor in the late phase. The tumor remained stationary during the following 6 months. The fam-ily history was negative for retinoblastoma.We diagnosed this case as an almost typical instance of retinoma or retinocytoma as described by Gallie and Zimmerman.

Rinsho Ganka (Jpn J Clin Ophthalmol) 41(6) : 685-688, 1987


Copyright © 1987, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1308 印刷版ISSN 0370-5579 医学書院

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